K-number	K130912
Device name	OMNICUT RESECTION BLADE
Applicant	Depuy Mitek, A Johnson & Johnson Company
Product code	HRX
Device class	Class II
Decision date	Jun 14, 2013
Decision	Substantially Equivalent
Regulation	888.1100

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Source

View the full FDA submission: accessdata.fda.gov

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OMNICUT RESECTION BLADE

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